吹扫捕集-气相色谱／质谱法测定水中25种挥发性有机物研究

建立了吹扫捕集与气相色谱／质谱联用测定水中25种挥发性有机物的分析方法。该方法的加标回收率在90％-119％之间,响应因子（RF）的相对标准偏差均小于20％,检出限在0．04μg／L-0．22μg／L之间。该方法具有简单、快速、准确、灵敏,无其他有机物的污染等优点,适用于地表水、地下水和饮用水中挥发性有机物的测定,结果令人满意。     

Influence of Chironomid Larvae on oxygen and nitrogen fluxes across the sediment-water interface (Lake Taihu, China)

The microscale distribution of oxygen,the nitrogen flux and the denitrification rates in sediment inhabited by chironomid larvae(Tanypus chinensis) were measured in eutrophic Lake Taihu,China.The presence of the chironomids in the sediment increased the oxygen diffusional flux from 10.4 ± 1.4 to 12.7 ± 2.5 mmol O 2 /(m 2 ·day).The burrows of the larvae represented "hot spots" and strongly influenced the nitrogen cycles and diagenetic activity in the sediment.The results indicate that the bioturbation effects of Tanypus chinensis chironomid larvae increased the capacity of the sediment as a sink for nitrate and a source for ammonium.Nitrate influx and ammonium outflux were increased 8.8 and 1.7 times,respectively.Under bioturbation,the amount of nitrate consumed was greater than the amount of ammonium released.The total denitrification rate was also enhanced from 0.76 ± 0.34 to 5.50 ± 1.30 mmol N/(m 2 ·day).The net effect was that the bioturbated sediments acted as a net sink for inorganic nitrogen under direct and indirect bioturbation effects compared to the control.     

Speciation of organic phosphorus in a sediment profile of Lake Taihu I: Chemical forms and their transformation

Organic phosphorus(nonreactive P,NRP)is a major component of P in sediments,but information about its chemical forms and dynamic transformation is limited.The chemical forms and dynamic behaviors of NRP in a sediment profile from Lake Taihu,a freshwater and eutrophic lake in China,were investigated.Five forms of NRP in the sediments were extracted based on a chemical fractionation technique,including easily labile NRP(NaHCO3-NRP),reactive metal oxide-bound NRP(HCl-NRP),humic acid-associated NRP(NaOH-NRPHA),fulvic acid-associated NRP(NaOH-NRPFA)and residual NRP(Res-TP).There were notable transformations with increasing sediment depth from the labile NaHCO3-NRP and NaOH-NRP pools to the recalcitrant HCl-NRP and Res-TP pools,which caused the NRP to become increasingly recalcitrant as the early diagenetic processes proceeded.Further analyses showed that the relative changes in contents of organic matter and reactive Fe oxides in the sediment profile triggered a competition for binding NRP fractions and led to the transformation of NRP.The results highlighted the importance of abiotic processes in regulating the diagenesis of organic P and its stability in sediments.     

吹扫捕集气质联用法测定水中4种挥发性有机物

建立了吹扫捕集气相色谱质谱联用法测定水中吡啶、丙烯腈、四乙基铅和松节油的方法,对吹扫时间进行了优化,研究了pH值对吹扫捕集率的影响。结果表明,在pH值为6¹0时,吹扫时间为11 min时吹扫捕集效率最高,用脉冲控制自动进标样的方法绘制工作曲线,曲线相关系数在0.99610时,吹扫时间为11 min时吹扫捕集效率最高,用脉冲控制自动进标样的方法绘制工作曲线,曲线相关系数在0.996⁰.999 9之间,方法的检出限在0.060.999 9之间,方法的检出限在0.06¹.0μg/L之间,相对标准偏差在1.1%1.0μg/L之间,相对标准偏差在1.1%⁶.2%之间,方法具有很好的线性和精密度。方法用于地表水、生活污水和化工废水中吡啶、丙烯腈、四乙基铅和松节油测定,并进行了加标回收实验,地表水回收率在86.8%6.2%之间,方法具有很好的线性和精密度。方法用于地表水、生活污水和化工废水中吡啶、丙烯腈、四乙基铅和松节油测定,并进行了加标回收实验,地表水回收率在86.8%¹12.1%之间,生活污水回收率在91.9%112.1%之间,生活污水回收率在91.9%⁹9%之间,废水回收率在82.2%～104.3%之间,表明方法具很好的准确度,可用于地表水、生活污水和化工废水中吡啶、丙烯腈、四乙基铅和松节油测定。     

自来水处理工艺对溶解相中全氟化合物残留的影响

为探究自来水原水到出厂水各处理环节对自来水中全氟化合物(perfluorinated compounds,PFCs)残留的影响,了解原水中PFCs的季节性变化规律,应用WAX固相萃取分离富集与高效液相色谱-质谱联用相结合的方法,分析了深圳市某自来水厂一年间原水、出厂水及絮凝池、沉降池、砂滤池、臭氧+活性炭池出水溶解相中13种PFCs的残留水平.结果表明,原水和出厂水中ΣPFCs残留呈春夏高而秋冬低的趋势,检出的PFCs呈中短链(C≤10)长链(C≥11)的分布,而全氟辛烷磺酸是PFCs最典型残留种态.在原水经过的5个处理环节中,臭氧+活性炭、沉降和砂滤具有PFCs去除效应,然而絮凝和液氯消毒却分别使短链(C≤6)和中链(10≥C≥7)PFCs显著上升,导致出厂水中ΣPFCs浓度较原水增加了10%～44%.但出厂水中PFCs残留远低于其限值,尚不足以影响人体健康.     

Determination of the mechanism of photoinduced toxicity of selected metal oxide nanoparticles (ZnO, CuO, Co3O4 and TiO2) to E. coli bacteria

Cytotoxicity of selected metal oxide nanoparticles(MNPs)(ZnO,CuO,Co 3 O 4 and TiO 2)was investigated in Escherichia coli both under light and dark conditions.Cytotoxicity experiments were conducted with spread plate counting and the LC 50 values were calculated.We determined the mechanism of toxicity via measurements of oxidative stress,reduced glutathione,lipid peroxidation,and metal ions.The overall ranking of the LC 50 values was in the order of ZnO < CuO < Co 3 O 4 < TiO 2 under dark condition and ZnO < CuO < TiO 2 < Co 3 O 4 under light condition.ZnO MNPs were the most toxic among the tested nanoparticles.Our results indicate depletion of reduced glutathione level and elevation of malondialdehyde level correlated with the increase in oxidative stress.Released metal ions were found to have partial effect on the toxicity of MNPs to E.coli.In summary,the dynamic interactions of multiple mechanisms lead to the toxicity of the tested MNPs to E.coli.     

环境空气中PM2.5与PM10质量浓度关系的研究

采集大连市4个大气自动监测点位30dPM2.5和PM10质量浓度小时值的监测数据,通过对每个点位720个有效数据对的统计分析,研究二者质量浓度的相关性及 PM2.5/PM10比值的分布情况,并研究了气象因素对PM2.5与PM10的影响。结果表明,雾使PM2.5PM10浓度都减小,但二者比值也随之降低;强风会使PM10浓度增大,但PM2.5浓度却减小。     

单偶氮染料AY17的光催化降解动力学及机制

为了研究水体环境中单偶氮染料酸性黄17(AY17)有效地去除方式及其可能的降解途径、转化和归趋等,实验首先探索了AY17在不同深度氧化体系中降解的可行性,研究发现其去除效率的大小按照UV/H_2O_2UV/Na_2S_2O_8≈UV/FeSO_4·7H_2OUV/KHSO_5UV/TiO_2排列.然后选取UV/TiO_2体系,研究了催化剂用量,反应温度,底物浓度以及溶液初始p H值等因素对其光催化降解动力学的影响,结果表明AY17的光催化降解遵循假一级动力学,其降解速率常数为0.011 2 min~(-1);当催化剂TiO_2用量为3 g·L~(-1)时其降解效果最好;高温有利于AY17的光催化降解,而随着底物浓度和溶液初始p H值的升高,其降解速率常数显著下降.最后利用GC/MS对AY17光催化降解中间产物进行了初步鉴定,研究发现在·OH等活性氧物种的作用下偶氮键的断裂、羟基自由基对芳香环上基团的取代以及吡唑环的裂解是其主要降解途径.     

超低溶解氧条件下的EBPR系统除磷性能

实验采用两个交替厌氧/好氧(An/O)模式运行的SBR反应器,对不同溶解氧(DO)浓度梯度下EBPR系统除磷效果及工艺性能进行了为期127 d的研究.在未控制DO的对照组反应器R1中,好氧段DO≥6 mg·L~(-1),运行的前65 d内工艺除磷性能稳定,除磷率95.9%,出水总磷0.5 mg·L~(-1),但由于系统长期处于过曝气状态,65 d后除磷性能逐渐恶化,直至97 d后系统彻底失效,整个运行阶段(1~127 d)出水总磷一级A达标率为39.4%.对于实验组反应器R2,控制好氧段DO浓度分别为2、1、0.5、0.2、0.1 mg·L~(-1),各工况初期除磷性能均有小幅波动,但除磷率迅速回升,继而反应器达到稳定运行.统计发现,实验组反应器R2在整个运行阶段出水总磷一级A的达标率为94.6%,127 d内仅有6 d不达标,工艺性能远优于R1.DO=2 mg·L~(-1)系统的比吸磷速率接近最大值,而低DO条件对比吸磷速率影响较大.实验还发现,尽管由超低DO(0.1 mg·L~(-1))引起的有机物降解速率低导致系统发生污泥微膨胀,但出水总磷仍能100%达标排放,微好氧EBPR的节能除磷具有可行性.     

我国自然生态系统氮沉降临界负荷评估

过量的氮沉降引起了一系列环境问题并导致生物多样性损失,因此评估当前生态系统氮沉降临界负荷对区域氮管理及其污染控制至关重要.利用稳态质量平衡法估算了当前我国自然生态系统的氮沉降临界负荷,并与氮沉降数据对比,获取了我国超过氮沉降临界负荷的生态系统空间分布情况.结果表明,6%的地区氮沉降临界负荷大于56 kg·(hm²·a)^-1,67%的地区氮沉降临界负荷在14～56 kg·(hm²·a)^-1之间,27%的地区氮沉降临界负荷小于14 kg·(hm²·a)^-1.氮沉降临界负荷较高的区域主要分布在青藏高原东部、内蒙古东北部和南部部分地区.氮沉降临界负荷较低的区域主要分布在青藏高原西部、西北地区和东南部分地区.氮沉降超过临界负荷的区域约占我国的21%,主要分布在东南和东北部分地区.东北、西北和青藏高原地区超临界负荷值普遍低于14 kg·(hm²·a)^-1.因此,未来这些超过氮沉降临界负荷地区的氮素管理和控制更为值得关注.